3-Butyn-1-OL → HCID 86755959, compound
Reaction equation
I[C:2]1[N:3]([CH2:16][C:17]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:20]=[CH:19][CH:18]=2)[CH:4]=[C:5]2[C:10]=1[CH2:9][N:8]([CH3:11])[CH2:7][N:6]2[CH2:12][CH:13]([CH3:15])[CH3:14].[CH2:27]([OH:31])[CH2:28][C:29]#[CH:30]>>[OH:31][CH2:27][CH2:28][C:29]#[C:30][C:2]1[N:3]([CH2:16][C:17]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[CH:20]=[CH:19][CH:18]=2)[CH:4]=[C:5]2[C:10]=1[CH2:9][N:8]([CH3:11])[CH2:7][N:6]2[CH2:12][CH:13]([CH3:14])[CH3:15]Participants
3
Procedure
The title compound was prepared from 5-iodo-3-methyl-1-(2-methylpropyl)-6-(1-naphthalenylmethyl )-1 H -pyrrolo[3,4-d]pyrimidine-2,4(3 H, 6 H)-dione and 3-butyn-1-ol in a manner analogous to the method of Example 13 above.
Sources & evidence
- ORD record
- ord-cc9589b02403449aa1e4ff378b2cbcf2
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06136974
Reaction notes
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